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Concept explainers
Interpretation:
The most stable chair conformation for the given compound has to be drawn.
Concept Introduction:
When a compound contains a cyclohexane ring in it, then there are three possibilities of conformations. They are chair, boat and twist-boat. Among these three conformations of cyclohexane ring, the most stable one is the chair conformation.
In the above structure, there are twelve substituents that can be placed. Among the twelve, six are axial substituents and six are equatorial substituents. The axial substituents can be represented as shown below,
The equatorial substituents can be represented as,
To draw a group in a correct configuration, we have to understand what is coming towards us and what is going away from us (wedge and dash bonds).
For drawing the other chair conformation, a ring flip has to be done. Ring flipping makes the skeleton as shown below,
During this ring flip from one chair conformation to another, all the substituents present in axial position goes to equatorial position and vice-versa.
The most stable conformation among the two chair conformations can be found by looking into the bulky groups that are present in the ring. The chair conformation which has the bulky group in equatorial position will be the more stable one as there wont be steric interaction. If the bulky group is present in axial position, then there will be axial-axial interaction, which makes the conformation less stable. In simple words, we can say that the bulky group will prefer to be in equatorial position.
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Chapter 6 Solutions
Organic Chemistry As a Second Language: First Semester Topics
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckGarrow_forwardThese are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forward
- Classify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forwardNonearrow_forwardQ4: Comparing (3S,4S)-3,4-dimethylhexane and (3R,4S)-3,4-dimethylhexane, which one is optically active? Briefly explain.arrow_forward
- Nonearrow_forwardNonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forward
- Determine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward
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